Hello all,
Thanks for looking to this thread. I really appreciate you for spending your valuable time for looking in to my thread and suggesting me to solve the problem. Let me introduce myself..
I am Kumar looking to find the NOC according to my job
I worked for 2 companies in Canada and each have different positions.
I found that both of my jobs are included in the NOC B, but unable to find the correct or nearly suitable NOC code.
1st company: Manufacturing of Natural Health products.
Position: Quality control Technician ( worked for 7 months)
Roles and Responsibilities:
· Perform Testing of Nutraceutical products and raw materials in support of corporate development projects and production support.
· Ensure all analytical results and documentation is of high quality, generated in a timely fashion that complies with GMP regulations and data integrity traceability requirements.
· Perform all in process testing’s in accordance with assigned specifications, methods or procedures.
· Review and prepare routine technical documents as directed.
· Perform all tasks in accordance with local policies and SOP’s.
· Maintain quality system records and collect documents.
· Review SOP’s, Batch Records, Equipment's, facility, utility, test methods and reports.
· Regularly update the Manager on test results, delays, problems and problems and process improvement recommendations.
· Holding all raw materials and finished products that fail to meet the established standards, and seek and finalize disposition on held items.
· Sampling of the Raw materials and send the samples to appropriate analytical labs.
· Ensure the Quality of product in all stages of Manufacturing.
· Involve in the Production and QC meetings to give the Qualitative output.
· In process checks for Tablets, Encapsulation, Packaging and checks during Sampling of Raw materials.
· Control and maintenance of raw material, finished product samples and their documents.
· Reporting all Deviation and problems to the management.
· Perform other duties as requested by Senior Management.
2nd Company: Manufacturing of Pharmaceutical Products and Natural Health Products.
Position: Quality Assurance Specialist
Roles and Responsibilities:
· As required, participate in examining the results, change controls requests when necessary, generate deviation reports, investigate root cause determination, and provide recommendation for corrective actions.
· Ensure Good Manufacturing practices (GMP) are carried out by all employees.
· Provide administrative support when required and ensuring compliance with all aspects of GMP regulations as required by Health Canada and the US FDA.
· Investigate, prepare reports on Customer complaints and respond in a timely manner.
· Review Certificate of analysis, Calibration reports, Batch manufacturing records, Batch Packaging records for any discrepancies, or errors, deviations and investigations (etc.) that could or may have the potential to impact the efficacy of the product.
· As required, contact customers and internal departments to respond to their inquiries and resolve QA issues.
· Prepare reports of Annual Product Review as per the clients request and respond to clients in a timely manner.
· Ensure to perform Risk Assessment using FMEA in every stage throughout the process when required.
· As required check all reports, records and data for completeness and accuracy as well as to confirm compliance with internal procedures and regulations.
· Check the New formulations that meet the specifications of customers and file related documents.
· Review of SOP’s, Bill of materials, customer signed PFSS documents and mange them in the ERP system.
Please help me in finding the correct or suitable NOC and help me to drop my PR File.
Thanks
Thanks for looking to this thread. I really appreciate you for spending your valuable time for looking in to my thread and suggesting me to solve the problem. Let me introduce myself..
I am Kumar looking to find the NOC according to my job
I worked for 2 companies in Canada and each have different positions.
I found that both of my jobs are included in the NOC B, but unable to find the correct or nearly suitable NOC code.
1st company: Manufacturing of Natural Health products.
Position: Quality control Technician ( worked for 7 months)
Roles and Responsibilities:
· Perform Testing of Nutraceutical products and raw materials in support of corporate development projects and production support.
· Ensure all analytical results and documentation is of high quality, generated in a timely fashion that complies with GMP regulations and data integrity traceability requirements.
· Perform all in process testing’s in accordance with assigned specifications, methods or procedures.
· Review and prepare routine technical documents as directed.
· Perform all tasks in accordance with local policies and SOP’s.
· Maintain quality system records and collect documents.
· Review SOP’s, Batch Records, Equipment's, facility, utility, test methods and reports.
· Regularly update the Manager on test results, delays, problems and problems and process improvement recommendations.
· Holding all raw materials and finished products that fail to meet the established standards, and seek and finalize disposition on held items.
· Sampling of the Raw materials and send the samples to appropriate analytical labs.
· Ensure the Quality of product in all stages of Manufacturing.
· Involve in the Production and QC meetings to give the Qualitative output.
· In process checks for Tablets, Encapsulation, Packaging and checks during Sampling of Raw materials.
· Control and maintenance of raw material, finished product samples and their documents.
· Reporting all Deviation and problems to the management.
· Perform other duties as requested by Senior Management.
2nd Company: Manufacturing of Pharmaceutical Products and Natural Health Products.
Position: Quality Assurance Specialist
Roles and Responsibilities:
· As required, participate in examining the results, change controls requests when necessary, generate deviation reports, investigate root cause determination, and provide recommendation for corrective actions.
· Ensure Good Manufacturing practices (GMP) are carried out by all employees.
· Provide administrative support when required and ensuring compliance with all aspects of GMP regulations as required by Health Canada and the US FDA.
· Investigate, prepare reports on Customer complaints and respond in a timely manner.
· Review Certificate of analysis, Calibration reports, Batch manufacturing records, Batch Packaging records for any discrepancies, or errors, deviations and investigations (etc.) that could or may have the potential to impact the efficacy of the product.
· As required, contact customers and internal departments to respond to their inquiries and resolve QA issues.
· Prepare reports of Annual Product Review as per the clients request and respond to clients in a timely manner.
· Ensure to perform Risk Assessment using FMEA in every stage throughout the process when required.
· As required check all reports, records and data for completeness and accuracy as well as to confirm compliance with internal procedures and regulations.
· Check the New formulations that meet the specifications of customers and file related documents.
· Review of SOP’s, Bill of materials, customer signed PFSS documents and mange them in the ERP system.
Please help me in finding the correct or suitable NOC and help me to drop my PR File.
Thanks